Gene >> HLA-C
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000376228 |
| Start |
31271851:31271851(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs281860324
|
| CDS Mutation |
c.91T>C |
| AA Mutation |
p.Tyr31His(p.Y31H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000376228 |
| Start |
31271647:31271647(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs41549514
|
| CDS Mutation |
c.295C>G |
| AA Mutation |
p.Arg99Gly(p.R99G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |